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A.I.M. KNOTLESS MENISCAL REPAIR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K133770
510(k) Type
Traditional
Applicant
ANCHOR INNOVATION MEDICAL (A.I.M.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2014
Days to Decision
181 days
Submission Type
Summary

A.I.M. KNOTLESS MENISCAL REPAIR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K133770
510(k) Type
Traditional
Applicant
ANCHOR INNOVATION MEDICAL (A.I.M.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/2014
Days to Decision
181 days
Submission Type
Summary